超麥特麥克羅斯 EUS 機器
K 號：K180731 · 2018-04-19
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器材摘要
Ultramatrix EUS Balloon is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc. (Us Endoscopy). It received FDA 510(k) clearance on 2018-04-19 under 510(k) number K180731. The device is classified under product code ODG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Ultramatrix EUS Balloon?
Ultramatrix EUS Balloon is a medical device that received FDA 510(k) clearance on 2018-04-19. The listed applicant is United States Endoscopy Group, Inc. (Us Endoscopy). The 510(k) number is K180731.
When did Ultramatrix EUS Balloon receive FDA 510(k) clearance?
Ultramatrix EUS Balloon received FDA 510(k) clearance on 2018-04-19, under 510(k) number K180731.
Who is the listed applicant for Ultramatrix EUS Balloon?
The FDA 510(k) record lists United States Endoscopy Group, Inc. (Us Endoscopy) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ultramatrix EUS Balloon?
The FDA product code for Ultramatrix EUS Balloon is ODG.
相關臨床試驗
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相關器械（代碼：ODG）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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